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Quentin Guigue

Publications and source records attributed to Quentin Guigue.

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Adhesion differentials control the rheology of biomimetic emulsions

Animal morphogenesis involves complex tissue deformation processes, which require tight control over tissue rheology. Yet, it remains insufficiently understood how tissue rheology results from the interplay between cellular packing and cellular forces, such as cortical tension, cell pressure, and cell-cell adhesion. Here, we follow a biomimetic approach to study this interplay. We mimic adhesive cells with oil droplets whose adhesion strength and specificity can be flexibly tuned. Using microfluidics, we expose 2D emulsions to an oscillatory geometry imposing cyclic pure shear, and we develop a geometric method to quantify their rheology using only imaging data. We find that some of the emulsions made of two droplet types progressively change their yielding behavior across subsequent shear cycles. Combining this with vertex model simulations, we show that the observed shift in yielding behavior is due to a progressive compaction, which only occurs in emulsions with a high adhesion differential and only when exposed to oscillatory shear. Gradients of cell compaction have been observed during animal development. Our work demonstrates how such gradients can be used to control gradients of tissue rheological properties. Moreover, the progressive compaction suggests the emergence of a pumping mechanism, which potentially acts in many cellular materials, from foams to tissues.

cond-mat.soft

Confinement controls bacterial spreading at all scales

Navigation of microorganisms is controlled by internal processes ultimately sensitive to mechanical or chemical signaling encountered along the path. In many natural environments, such as porous soils or physiological ducts, motile species alternate between bulk and surface motion displaying in each case, distinct kinematics. This inherent complexity is key to many practical biological and ecological issues involving spreading and contamination, essential for understanding the spatiotemporal structuring of populations in their environment. However grasping the interplay between geometrical confinement and kinematics driven by internal biological responses remains poorly understood from a physical and biological standpoint. Here, we address this question through experimental and theoretical analysis in the heuristic situation of two parallel confining surfaces. We track wild-type E. coli - a model peritrichous flagellated bacterium - in 3D over extended periods of time. We obtain the first experimental measurements of the emerging diffusivity and bulk/surface residence times as a function of confinement height and the specific chiral kinematics at surfaces. All experimental results are quantitatively reproduced, without parametric adjustment, by a non-Markovian stochastic (BV) model that incorporates the internal biochemical memory carried by a phosphorylated protein switching the motor rotation. By matching the results with a Markovian (memoryless) companion model, we derive an analytical expression for the diffusivity and demonstrate how confining walls influence microbial long-range dispersion. This approach also provides a general conceptual basis for understanding how microorganisms navigate complex environments, in which their movement alternates between bulk and surfaces.

physics.bio-ph